CRA II, Norway

Job description

This role is for upcoming future opportunities that may arise at Fortrea. It is a full-time position supporting a single sponsor. Role is based in the Oslo area. Key requirement: Minimum 2 years of clinical monitoring experience Preferably 1+ year experience in oncology studies Summary of Responsibilities: Manage clinical trial sites in line with Fortrea SOPs, ICH GCP and sponsor requirements Perform all monitoring visits (PSV, SIV, routine, close-out) Ensure patient safety by verifying informed consent and protocol adherence Maintain data integrity through SDV, query management, and data review Keep site regulatory documentation and eTMF up to date Oversee investigational product handling, storage, and accountability Ensure audit readiness and compliance with quality standards and CRA metrics Prepare monitoring plans, visit reports, and study documentation On-site Monitoring Responsibilities: Ensure site staff are trained and equipped to run the study Verify subject eligibility, consent, and protocol compliance Review source data for accuracy and completeness Identify and resolve data discrepancies and deviations Perform efficient monitoring activities in line with SOPs and travel...